Orbital schwannoma with hyposmia as the only presentation: Case report and a literature review on differential diagnosis

2021 ◽  
pp. 014556132110598
Author(s):  
Xiangyu Lou ◽  
Bo Jiang ◽  
Jianguang Zhong ◽  
Jian Wu ◽  
Haibin Wang ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Preoperative Diagnosis ◽  
Benign Tumor ◽  
Mri Imaging ◽  
Resonance Imaging ◽  
Nerve Sheath ◽  
Rare Benign Tumor ◽  
Combined Imaging ◽  
Magnetic Resonance Imaging Mri ◽  
Atypical Presentations

Orbital schwannoma is a rare benign tumor, originating from the Schwann cells of the orbital peripheral nerve sheath. Orbital schwannoma is easily misdiagnosed if the patient shows atypical presentations and atypical appearance on MRI imaging. A 56-year-old male experienced hyposmia for 1 year and was misdiagnosed with cavernous hemangioma pre-operation. This case was treated by surgery through the endoscopic trans-nasal approach. After operation, the patient had no recurrence or complications. Preoperative diagnosis for these cases remains difficult. Combined imaging modalities including computed tomography (CT) and magnetic resonance imaging (MRI) can help in differential diagnosis. Surgery is the main treatment modality for treating orbital schwannoma. Outcomes in most cases are favorable without complications or recurrence.

Pelvic Schwannoma: Robotic Laparoscopic Resection

2012 ◽  
Vol 72 (1) ◽  
pp. ons2-ons5 ◽  
Author(s):  
Constance Deboudt ◽  
Jean-Jacques Labat ◽  
Thibault Riant ◽  
Olivier Bouchot ◽  
Roger Robert ◽  
...  
Keyword(s):  
Peripheral Nerves ◽  
Benign Tumor ◽  
Laparoscopic Resection ◽  
Resonance Imaging ◽  
Pelvic Nerve ◽  
Neurological Sequelae ◽  
Nerve Sheath ◽  
Rare Benign Tumor ◽  
The Right

Abstract Background: Schwannoma is a rare benign tumor of peripheral nerves arising from Schwann cells of the ubiquitous nerve sheath. Objective: To describe the operative steps and technical aspects of robotic laparoscopic resection of pelvic schwannoma. Methods: We describe 2 patients with pelvic schwannoma: a 34-year-old woman with schwannoma of the right lumbosacral trunk and a 58-year-old woman with schwannoma of a left S1 nerve. Pain was the main symptom in both patients. The diagnosis was confirmed by magnetic resonance imaging and nerve biopsies. Both patients were operated on by robotic laparoscopy. Results: Lesions were totally enucleated after incising the epineurium. After dissection of the schwannoma, the vascular pedicle and nerve fascicles involved were identified, coagulated, and then sectioned. The remaining fascicles of the nerve were preserved. The postoperative course was uneventful in both patients. With follow-up of 9 and 13 months, both patients obtained complete pain relief with no neurological sequelae. Conclusion: Robotic laparoscopic resection of pelvic nerve tumors such as schwannomas is technically feasible.

Facial Nerve Angioma

1996 ◽  
Vol 75 (4) ◽  
pp. 225-238 ◽  
Author(s):  
Jack L. Pulec
Keyword(s):  
Facial Nerve ◽  
Benign Tumor ◽  
Nerve Grafting ◽  
Total Excision ◽  
Resonance Imaging ◽  
Rare Benign Tumor ◽  
Permanent Cure ◽  
Magnetic Resonance Imaging Mri ◽  
Lesion Treatment ◽  
Facial Function

Angioma of the facial nerve is a rare benign tumor. Symptoms include progressive or sudden facial paralysis and, often, a facial twitch. Although angiomas have unique features, diagnosis and treatment is similar to that for facial nerve neuroma. Magnetic Resonance Imaging (MRI) with gadolinium infusion and thin-section Computed Tomography (CT) can often identify the lesion. Treatment by total excision and facial nerve grafting can provide a permanent cure with good restoration of facial function. Four cases are discussed.

scholarly journals Pulvinar sign in a case of anti-HU paraneoplastic encephalitis

2016 ◽  
Vol 29 (6) ◽  
pp. 436-439 ◽  
Author(s):  
Pierre-Luc Gamache ◽  
Maude-Marie Gagnon ◽  
Martin Savard ◽  
François Émond
Keyword(s):  
Magnetic Resonance Imaging ◽  
Differential Diagnosis ◽  
Magnetic Resonance ◽  
Clinical Manifestations ◽  
Resonance Imaging ◽  
Paraneoplastic Encephalitis ◽  
Jakob Disease ◽  
Magnetic Resonance Imaging Mri ◽  
Work Up

This article reports the case of a 68-year-old patient with anti-HU antibodies paraneoplastic encephalitis. The clinical manifestations were atypical and the paraclinical work-up, notably the magnetic resonance imaging (MRI) showing bilateral posterior thalamic hyperintensities (pulvinar sign), misleadingly pointed towards a variant Creutzfeld–Jakob disease. After presenting the case, the differential diagnosis of the pulvinar sign is discussed along with other important diagnostic considerations.

scholarly journals Laparoscopic Resection of a Giant Dedifferentiated Primary Retroperitoneal Mucinous Cystadenoma (PRMC) in a Young Woman: A Case Report and Literature Review

2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Wu L ◽  
Li X ◽  
Li J ◽  
Lai Y
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Literature Review ◽  
Benign Tumor ◽  
Laparoscopic Resection ◽  
Abdominal Cavity ◽  
Mucinous Cystadenoma ◽  
Rare Benign Tumor ◽  
Primary Retroperitoneal

Background: PRMC is a very rare benign tumor of the abdominal cavity that usually occurs in women, and PRMC demonstrate no specific findings on CT. There are many reports on the differential diagnosis and discussion of PRMC imaging, but there are few reports on the treatment of dedifferentiated PRMC using laparoscopic resection and postoperative follow-up.

scholarly journals Mastoid Bone involved by Pleomorphic Adenoma

2016 ◽  
Vol 8 (3) ◽  
pp. 111-112
Author(s):  
Pradipta K Parida
Keyword(s):  
Magnetic Resonance Imaging ◽  
Magnetic Resonance ◽  
Parotid Gland ◽  
Pleomorphic Adenoma ◽  
Surgical Planning ◽  
Benign Tumor ◽  
Review Of Literature ◽  
Resonance Imaging ◽  
Mastoid Bone ◽  
Magnetic Resonance Imaging Mri

ABSTRACT Pleomorphic adenoma is a benign tumor of the salivary glands, most commonly affecting the parotid gland. Pleomorphic adenoma of the ear is rare. The use of imaging modalities, especially magnetic resonance imaging (MRI), is particularly useful in localizing and surgical planning of these tumors. We present a case of pleomorphic adenoma invading the mastoid cortical bone, with review of literature. How to cite this article Vamanshankar H, Parida PK. Mastoid Bone involved by Pleomorphic Adenoma. Int J Otorhinolaryngol Clin 2016;8(3):111-112.

scholarly journals Diagnostic value of magnetic resonance imaging in the analysis of ameloblastoma: report of two cases

2019 ◽  
Vol 22 (3) ◽  
pp. 425-431
Author(s):  
Neiandro Santos Galvão ◽  
Antonione Santos Bezerra Pinto ◽  
Alan Leandro Carvalho Farias ◽  
André Luiz Ferreira Costa ◽  
Sérgio Lúcio Pereira de Castro Lopes ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Differential Diagnosis ◽  
Magnetic Resonance ◽  
Signal Intensity ◽  
Diagnostic Value ◽  
Resonance Imaging ◽  
Intermediate Signal Intensity ◽  
Additional Information ◽  
Imaging Characteristics ◽  
Magnetic Resonance Imaging Mri

Ameloblastoma is an odontogenic tumor that shares clinical and imaging characteristics with other lesions of the jaws, such as odontogenic keratocyst, which makes the diagnosis difficult. However, in addition to radiographic and tomographic examinations, Magnetic Resonance Imaging (MRI) has been increasingly used, contributing with relevant additional information about the differentiation between solid and liquid components of the lesion. This case report was conducted to present two variations of ameloblastoma and discuss the radiographic, tomographic and MRI contribution in the differential diagnosis between ameloblastoma and odontogenic keratocyst.The signal intensity in T1-weighted MRI revealed internal fluid content in both cases, which was important in the differential diagnosis with other intraosseous lesions such as odontogenic keratocysts. This is probably due to the presence of keratin that increases the viscosity of the content and also for an intermediate signal intensity signal in T2-weighted MRI. Therefore, MRI revealed important internal characteristics of the reported lesions, which was very useful in the establishment of the differential diagnosis with other lesions.

Surgical Excision of a Cavernous Hemangioma of the Rostral Brain Stem: Case Report

Neurosurgery ◽  
1988 ◽  
Vol 23 (4) ◽  
pp. 490-493 ◽  
Author(s):  
Stephen L. Ondra ◽  
James R. Doty ◽  
Michael E. Mahla ◽  
Eugene D. George
Keyword(s):  
Magnetic Resonance Imaging ◽  
Case Report ◽  
Brain Stem ◽  
Cavernous Hemangioma ◽  
Preoperative Diagnosis ◽  
Surgical Techniques ◽  
Surgical Excision ◽  
Resonance Imaging ◽  
Mri Findings ◽  
Magnetic Resonance Imaging Mri

Abstract A 23-year-old pregnant woman presented with sudden diplopia, ataxia, hemiparesis, and headache secondary to a brain stem hemorrhage. Magnetic resonance imaging (MRI) revealed a hematoma associated with a probable cavernous hemangioma of the rostral brain stem. In this report, we discuss the MRI findings leading to the preoperative diagnosis, as well as the surgical techniques involved in the successful resection.

Meningioma in the internal auditory canal

2001 ◽  
Vol 115 (1) ◽  
pp. 48-49 ◽  
Author(s):  
P. Martinez Devesa ◽  
M. J. Wareing ◽  
D. A. Moffat
Keyword(s):  
Magnetic Resonance Imaging ◽  
Differential Diagnosis ◽  
Magnetic Resonance ◽  
Histological Examination ◽  
Vestibular Schwannoma ◽  
Internal Auditory Canal ◽  
Resonance Imaging ◽  
Translabyrinthine Approach ◽  
Magnetic Resonance Imaging Mri

A case is presented of an entirely intracanalicular meningioma in a 48-year-old woman that was excised via a conventional translabyrinthine approach to the internal auditory canal (IAC). Pre-operative magnetic resonance imaging (MRI) suggested that the tumour was a vestibular schwannoma (VS). Histological examination confirmed the intra-operative impression that the tumour was a meningioma. Although VS is by far the commonest intracanalicular tumour, the differential diagnosis includes meningioma. MRI is unable to distinguish between these two entities when the tumour is located entirely in the internal auditory canal.

scholarly journals A case report of lymphocytic hypophysitis

2021 ◽  
Vol 12 ◽  
pp. 263
Author(s):  
Stephen Yu ◽  
Ramakrishna Bethanabatla ◽  
Ahmed Taha
Keyword(s):  
Differential Diagnosis ◽  
Rare Condition ◽  
Lymphocytic Hypophysitis ◽  
Reproductive Age ◽  
Case Description ◽  
Clinical Correlation ◽  
Resonance Imaging ◽  
Sellar Mass ◽  
Mri Findings ◽  
Magnetic Resonance Imaging Mri

Background: Lymphocytic hypophysitis (LH) is a rare condition that mostly affects women of the reproductive age. Because it is infrequently encountered, it is not often considered as a differential diagnosis of sellar masses. The diagnosis is made clinically with the aid of magnetic resonance imaging (MRI) and should be considered if the patient has endocrine derangements in addition to a sellar mass. Case Description: A 37-year-old female presents with a complaint of headaches and CT imaging showed a sellar mass. She was also being investigated simultaneously by the endocrine department and was diagnosed with panhypopituitarism. She proceeded to surgery for a presumed pituitary adenoma but histopathology returned as LH. Conclusion: It is important to have a wide differential diagnosis when managing pituitary masses. Clinical correlation with atypical MRI findings is useful to determine the diagnosis of LH.

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